scholarly journals Tu1737 – Efficacy of the Anti-Mucosal Addressin Cell Adhesion Molecule-1 (MADCAM-1) Antibody Shp647 in Ulcerative Colitis: Results from the Open-Label Extension Study Turandot Ii

2019 ◽  
Vol 156 (6) ◽  
pp. S-1105
Author(s):  
Walter Reinisch ◽  
William J. Sandborn ◽  
Silvio Danese ◽  
Xavier Hebuterne ◽  
Maria Klopocka ◽  
...  
Author(s):  
Nathalie Van den Berghe ◽  
Bram Verstockt ◽  
Ann Gils ◽  
João Sabino ◽  
Marc Ferrante ◽  
...  

Abstract Background and aims Some patients with ulcerative colitis (UC) do not respond to vedolizumab treatment despite adequate drug exposure in serum. This study aimed to investigate vedolizumab in tissue and questioned whether insufficient tissue exposure could explain non-response in UC patients with adequate serum vedolizumab concentrations. Methods A paired serum sample and colonic mucosal biopsy was collected from 40 UC patients (20 endoscopic responders, 20 non-responders) at week 14 of vedolizumab treatment. Vedolizumab, soluble (s)-mucosal addressin cell adhesion molecule-1 (MAdCAM-1), s-vascular cell adhesion molecule-1 (VCAM-1) and s-intercellular adhesion molecule-1 (ICAM-1) were measured in serum and/or tissue. Endoscopic response was defined as Mayo endoscopic sub-score ≤1. Results A significant positive correlation was observed between vedolizumab serum and colonic tissue concentrations (ρ = 0.84, p<0.0001), regardless of the macroscopic inflammatory state of the tissue. Vedolizumab tissue concentrations were lower in non-responders than in responders (0.07 vs 0.11 µg/mg, p = 0.04). In the subgroup of patients with adequate vedolizumab serum concentrations (>14.6 µg/mL), tissue vedolizumab was not significantly different between responders and non-responders (0.15 vs 0.13 µg/mg; p = 0.92). Serum sMAdCAM-1, but not serum sICAM-1 or sVCAM-1 concentrations, were significantly higher in responders than non-responders with adequate vedolizumab serum concentrations (1.04 vs 0.83 ng/mL, p =0.03). Conclusions Vedolizumab concentrations in colonic mucosal tissue of UC patients reflect the concentration in serum regardless of the macroscopic inflammatory state of the tissue. Our data shows that insufficient tissue exposure does not explain non-response in UC patients with adequate serum vedolizumab concentrations.


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